1979
DOI: 10.7164/antibiotics.32.679
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New antibiotic pigments related to fusarubin from Fusarium solani (MART.) SACC. I. Fermentation, islation, and antimicrobial activities.

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Cited by 27 publications
(20 citation statements)
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“…Of those tested, most have exhibited activity against grampositive bacteria, with MIC values from 2 to 500 ~tg mL (Table 3). A comparison of published MIC values for S. aureus to those of the present study showed our culture was less sensitive to compound 7 (bostrycoidin), but more sensitive to compounds 6 and 18 (anhydrofusarubin and javanicin) [ 1,5].…”
Section: Resultssupporting
confidence: 51%
“…Of those tested, most have exhibited activity against grampositive bacteria, with MIC values from 2 to 500 ~tg mL (Table 3). A comparison of published MIC values for S. aureus to those of the present study showed our culture was less sensitive to compound 7 (bostrycoidin), but more sensitive to compounds 6 and 18 (anhydrofusarubin and javanicin) [ 1,5].…”
Section: Resultssupporting
confidence: 51%
“…Increased expression of 5-methyltetrahydropteroyltriglutamate homocysteine methyltransferase, MetE (BGLT01007) in co-cultivation with A. alternaria also suggests oxidative stress, since this protein is very highly expressed in E. coli cells exposed to oxidative stress (Hondorp and Matthews, 2004). Antibacterial compounds released by the fungi could cause oxidative stress (Ammar et al, 1979;Hellwig et al, 2002;Deshmukh et al, 2014;Soltani and Hosseyni Moghaddam, 2014). An increase of the RND (resistance nodulation division) family of efflux pumps (Rivilla et al, 1995) and the CmeABC multidrug efflux system of Campylobacter jejuni (Lin et al, 2002), which are involved in the export of a wide range of drugs.…”
Section: Genetic Features Of B Glathei Lgm14190 Possibly Involved Inmentioning
confidence: 99%
“…nHexane soluble fraction was obtained only in three strains which showed mild toxicity. Antimicrobial naphthoquinones are widely distributed in plants, fungi and some animals (Riffel et al, 2002) are also reported from F. solani (Ammar et al, 1979;Baker et al, 1990). Besides naphthoquinones, F. solani is also known to produce diterpene and paclitaxel (Chakravarthi et al, 2008), and has been used alone or in combination with other chemotherapeutic agents for the treatment of variety of cancers, as well as AIDS-related Kaposi sarcoma (Brown, 2003;Croom, 1995 Means of 3 replicates.…”
Section: Resultsmentioning
confidence: 99%
“…F. solani is known to produce naphthoquinone compounds (Baker et al, 1990) including fusarubin, anhydrofusarubin, javanicin, norjavanicin, methyl etherfusarubin, marticin, isomarticin, bostrycoidia, ethyl ether-fusarubin, solaniol, nectriafusarubin and dihydrofusarubin lactone (James & Robert 1983;Kurobane et al, 1980;Tatum et al, 1985). Some naphthaquinones have antimicrobial, toxic, insecticidal and antitumor properties (Ammar et al, 1979). In our previous study, F. solani strains showed nematicidal activity against Meloidogyne javanica (Hameed et al, 2001) and antimicrobial activity against some Gram positive and negative bacteria and root rot strain of F. solani (Qureshi et al, 2003).…”
mentioning
confidence: 99%